This week we
George’s sister is training a new caregiver for mom. This new caregiver will work from 4-8PM five
days a week (Monday through Friday). It
was inevitable that more caregivers would be added to assist with mom. George’s health issue has forced us into
transitioning to the next care phase for mom sooner than we expected. It is not unwelcome, but it is a change for
everyone.
We have been
telling mom for about a week that there would be a new caregiver in her
life. She has been fighting us tooth and
nails on this issue insisting that she is just fine by herself. She has been cranky, combative, crying. Just minutes prior to the caregiver arriving
for the first time she had been arguing with Rosemary. Then, when the caregiver arrived, she jumped
up and hugged her and told her it was nice to see her again (though she has
never met her before). I call this the
Dr. Jekyll/Mr. Hyde syndrome she has.
She will be gnarly with us and turn around to her caregivers and daycare
and turn on the sugar. It can be quite
frustrating!
Having added
caregivers will enable George and I to have a little more down time, time to go
out for dinners, time to sit and relax, take a walk. It should reduce my stress
level just a tad bit. This will have
more impact on me since I am the one used to jumping up every twenty to thirty
minutes to make sure she has her dinner and her medications, make sure that she
is not doing things she should not be doing. It is a strange feeling to have
some of the load lifted. I am not used
to just sitting down in the evenings with no place to go. I don’t know what I will do with all this
extra time! I am sure I will get used to
it.
For now it
will allow me to go play my monthly Bunco (like tonight) – without having to
remind George what does or does not need to be done. It will enable us to have dinner out with
friends or just go out on our own and not have to rush home. We can even run
out and do some shopping!
In a few
weeks it will give me the time I need to concentrate on George’s healing from
surgery. That will be my primary focal
point for a while.
We are
fortunate that George’s sister will be able to step up to the plate and handle
the other “off hours” (8PM to 7AM) for the times that I need to be away from
home or when I need the extra sleep.
This period
of time will be all about allowing others to step up and help where it is
needed. In a “I can do it myself” world, this is a hard change to make. Necessary, but still hard. There will be more
changes ahead – even if there was no cancer in our world there would be more
changes – and we will need to adapt to those changes in our lives like shifting
sand . . . as gracefully as we possibly can.
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